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Theorem 4 Let S M be a monogenic semigroup as given in (1).
Theorem 8 Let S M be a monogenic semigroup as in (1).
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For a monogenic semigroup S M as in (1), the chromatic number of the graph Γ ( S M ) is given by 1 + ⌈ n − 1 2 ⌉.
It is a monogenic disease caused by mutations in the gene encoding the dystrophin protein.
Familial hypercholesterolemia is a monogenic disorder caused by mutations in the LDL receptor (LDLR) gene.
SCCOHT is a monogenic disease, characterized by germline and somatic SMARCA4 mutations.
Then, is a monogenic extension of to, which obviously belongs to.
In certain families, FHM is a monogenic disorder distinct from migraine with typical aura.
Familial hemiplegic migraine (FHM) is a monogenic subtype of migraine with aura.
Familial hemiplegic migraine is a monogenic disorder that is distinct from migraine with typical aura.
SCD is a monogenic, hematological and multi-organ disorder associated acute and chronic illness, and progressive organ damage [2].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com